EP2537946B1 - Procédé de fabrication d'une tôle d'acier électrique à grains orientés - Google Patents
Procédé de fabrication d'une tôle d'acier électrique à grains orientés Download PDFInfo
- Publication number
- EP2537946B1 EP2537946B1 EP11744741.7A EP11744741A EP2537946B1 EP 2537946 B1 EP2537946 B1 EP 2537946B1 EP 11744741 A EP11744741 A EP 11744741A EP 2537946 B1 EP2537946 B1 EP 2537946B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- mass
- steel sheet
- annealing
- temperature
- grain
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 229910001224 Grain-oriented electrical steel Inorganic materials 0.000 title claims description 40
- 238000004519 manufacturing process Methods 0.000 title claims description 15
- 238000000034 method Methods 0.000 title description 14
- 238000000137 annealing Methods 0.000 claims description 128
- 229910000831 Steel Inorganic materials 0.000 claims description 108
- 239000010959 steel Substances 0.000 claims description 108
- 238000005261 decarburization Methods 0.000 claims description 42
- 238000005097 cold rolling Methods 0.000 claims description 20
- 239000010960 cold rolled steel Substances 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 16
- 238000005098 hot rolling Methods 0.000 claims description 15
- 229910052802 copper Inorganic materials 0.000 claims description 13
- 238000010438 heat treatment Methods 0.000 claims description 13
- 238000005121 nitriding Methods 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 239000012535 impurity Substances 0.000 claims description 8
- 229910052718 tin Inorganic materials 0.000 claims description 8
- 229910052748 manganese Inorganic materials 0.000 claims description 7
- 229910052698 phosphorus Inorganic materials 0.000 claims description 7
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- 229910052804 chromium Inorganic materials 0.000 claims description 5
- 229910052797 bismuth Inorganic materials 0.000 claims description 3
- 229910052745 lead Inorganic materials 0.000 claims description 3
- 229910052750 molybdenum Inorganic materials 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 229910052711 selenium Inorganic materials 0.000 claims description 3
- 229910052720 vanadium Inorganic materials 0.000 claims description 3
- 229910052787 antimony Inorganic materials 0.000 claims 2
- 238000001953 recrystallisation Methods 0.000 description 30
- 230000004907 flux Effects 0.000 description 20
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- 238000002474 experimental method Methods 0.000 description 18
- 239000002244 precipitate Substances 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
- 239000013078 crystal Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 7
- 239000003112 inhibitor Substances 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 229910021529 ammonia Inorganic materials 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 229910000976 Electrical steel Inorganic materials 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 238000005554 pickling Methods 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- 238000005266 casting Methods 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/12—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D3/00—Diffusion processes for extraction of non-metals; Furnaces therefor
- C21D3/02—Extraction of non-metals
- C21D3/04—Decarburising
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/04—Making ferrous alloys by melting
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/001—Ferrous alloys, e.g. steel alloys containing N
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/008—Ferrous alloys, e.g. steel alloys containing tin
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/14—Ferrous alloys, e.g. steel alloys containing titanium or zirconium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/16—Ferrous alloys, e.g. steel alloys containing copper
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/34—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of silicon
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/02—Pretreatment of the material to be coated
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/80—After-treatment
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
- H01F1/14—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys
- H01F1/16—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys in the form of sheets
Definitions
- the present invention relates to a method of manufacturing a grain-oriented electrical steel sheet in which the variation in magnetic property is suppressed.
- a grain-oriented electrical steel sheet is a steel sheet which contains Si and in which crystal grains are highly integrated in a ⁇ 110 ⁇ 001> orientation, and is used as a material of a wound core of a stationary induction apparatus such as a transformer.
- the control of the orientation of the crystal grains is conducted with catastrophic grain growth phenomenon called secondary recrystallization.
- heating is performed on a slab at a temperature of 1280°C or higher to almost completely solid-solve fine precipitates called inhibitors, and thereafter hot rolling, cold rolling, annealing and so on are performed to cause the fine precipitates to precipitate during the hot rolling and the annealing.
- heating is performed on a slab at a temperature of lower than 1280°C, and thereafter hot rolling, cold rolling, decarburization annealing, nitriding, finish annealing and so on are performed to cause AlN (Al, Si)N and the like to precipitate as inhibitors during the nitriding.
- the former method is sometimes called a high-temperature slab heating method, and the latter method is sometimes called a low-temperature slab heating method.
- nitridation annealing is normally performed after decarburization annealing also serving as primary recrystallization annealing is performed, and the decarburization annealing and the nitridation annealing are tried to be simultaneously performed in recent years. If it becomes possible to simultaneously perform the decarburization annealing and the nitridation annealing, it becomes possible to perform them in one furnace and use existing annealing facilities, and to reduce the total treatment time required for annealing and suppress the energy consumption.
- An object of the present invention is to provide a method of manufacturing a grain-oriented electrical steel sheet, capable of suppressing the variation in magnetic property.
- the conceivable reason why the crystal grains do not uniformly grow is that when the decarburization annealing and the nitridation annealing are simultaneously performed, the primary recrystallization and the nitridation proceed during the decarburization annealing, thereby causing a difference in size of a precipitate in the thickness direction of the steel sheet. More specifically, the primary recrystallized grain is less likely to grow on the surface layer portion of the steel sheet due to the formation of the precipitate with the nitridation, whereas the primary recrystallized grain is more likely to grow at the central portion because the precipitate is not formed before a certain amount of nitrogen diffuses. Accordingly, it is conceivable that there occurs variation in the grain diameter of the primary recrystallized grain to make the grain diameter (secondary recrystallization grain diameter) obtained through secondary recrystallization nonuniform, resulting in a large variation in magnetic property.
- the present inventors thought, based on such knowledge, that it is possible to uniformly cause the secondary recrystallization through forming an effective precipitate in order to make the crystal grain growth uniform during the finish annealing in the low-temperature slab heating method in which the decarburization annealing and the nitridation annealing are simultaneously performed. Then, the present inventors repeatedly carried out an experiment of measuring the magnetic properties of the grain-oriented electrical steel sheets obtained through adding various kinds of elements to slabs. As a result, the present inventors found that addition of Ti and Cu was effective to make the secondary recrystallization uniform.
- the present inventors repeatedly conducted the experiments of measuring the magnetic properties of grain-oriented electrical steel sheets obtained through adding various kinds of elements to slabs and found out that addition of Ti and Cu is effective to make the secondary recrystallization uniform.
- silicon steel with a composition used for manufacturing a grain-oriented electrical steel sheet based on a low-temperature slab heating method was used, for example. Further, Ti and Cu were contained at various ratios into the silicon steel to produce steel ingots with various compositions. Further, the steel ingots were heated at a temperature of 1250°C or lower and subjected to hot rolling, and then subjected to cold rolling. Furthermore, decarburization annealing and nitridation annealing were simultaneously performed after the cold rolling, and then finish rolling was performed. Then, the magnetic flux densities B8 of the obtained grain-oriented electrical steel sheets were measured and the variations in the magnetic flux densities B8 in coils after the finish annealing were checked.
- the magnetic flux density B8 is the magnetic flux density occurring in the grain-oriented electrical steel sheet when a magnetic field of 800 A/m at 50 Hz is applied thereto.
- Fig. 1 An example of the results obtained through the above-described experiments is illustrated in Fig. 1 .
- an open circle mark in Fig. 1 indicates that the average value of the magnetic flux densities B8 of five single-plate samples was 1.90 T or more and the difference between the maximum value and the minimum value of the magnetic flux density B8 was 0.030 T or less.
- a filled circle mark in Fig. 1 indicates that at least the average value of the magnetic flux densities B8 of five single-plate samples was less than 1.90 T or the difference between the maximum value and the minimum value of the magnetic flux density B8 was more than 0.030 T. It is apparent from Fig.
- FIG. 2 is a flowchart illustrating the method of manufacturing a grain-oriented electrical steel sheet according to the embodiment of the present invention.
- a slab is produced through casting of molten steel for a grain-oriented electrical steel sheet with a predetermined composition (Step 1).
- the casting method therefor is not particularly limited.
- the molten steel contains, for example, Si: 2.5 mass% to 4.0 mass%, C: 0.02 mass% to 0.10 mass%, Mn: 0.05 mass% to 0.20 mass%, acid-soluble Al: 0.020 mass% to 0.040 mass%, N: 0.002 mass% to 0.012 mass%, S: 0.001 mass% to 0.010 mass%, and P: 0.01 mass% to 0.08 mass%.
- the molten steel further contains at least one kind selected from a group consisting of Ti: 0.0020 mass% to 0.010 mass% and Cu: 0.010 mass% to 0.50 mass%.
- the molten steel contains one or both of Ti and Cu in ranges of Ti: 0.010 mass% or less and Cu: 0.50 mass% or less to satisfy at least one of Ti: 0.0020 mass% or more or Cu: 0.010 mass% or more.
- the balance of the molten steel may be composed of Fe and inevitable impurities. Note that the inevitable impurities may include an element(s) forming an inhibitor in the manufacturing process of the grain-oriented electrical steel sheet and remaining in the grain-oriented electrical steel sheet after purification is performed through high-temperature annealing.
- Si is an element that is extremely effective to enhance the electrical resistance of the grain-oriented electrical steel sheet to reduce the eddy current loss constituting a part of the core loss.
- the Si content is less than 2.5 mass%, the eddy current loss cannot be sufficiently suppressed.
- the Si content is more than 4.0 mass%, the processability is lowered. Accordingly, the Si content is set to 2.5 mass% to 4.0 mass%.
- C is an element that is effective to control the structure (primary recrystallization structure) obtained through primary recrystallization.
- the C content is less than 0.02 mass%, the effect cannot be sufficiently obtained.
- the C content is more than 0.10 mass, the time required for decarburization annealing increases, resulting in a larger exhaust amount of CO 2 .
- the C content is set to 0.02 mass% to 0.10 mass%.
- the embodiment is particularly effective in the case where the C content is 0.06 mass% or less.
- Mn increases the specific resistance of the grain-oriented electrical steel sheet to reduce the core loss. Mn also functions to prevent occurrence of cracks in the hot rolling. When the Mn content is less than 0.05 mass%, the effects cannot be sufficiently obtained. On the other hand, when the Mn content is more than 0.20 mass%, the magnetic flux density of the grain-oriented electrical steel sheet is lowered. Accordingly, the Mn content is set to 0.05 mass% to 0.20 mass%.
- Acid-soluble Al is an important element forming AlN serving as an inhibitor.
- the acid-soluble Al content is less than 0.020 mass%, a sufficient amount of AlN cannot be formed, resulting in insufficient inhibitor strength.
- the acid-soluble Al content is more than 0.040 mass%, AlN becomes coarse, resulting in a decrease in inhibitor strength. Accordingly, the acid-soluble Al content is set to 0.020 mass% to 0.040 mass%.
- N is an important element forming AlN through reacting with the acid-soluble Al. Though a large amount of N does not need to be contained in the grain-oriented electrical steel sheet because nitridation annealing is performed after the cold rolling as will be described later, a great load may be required in steelmaking in order to make the N content less than 0.002 mass%. On the other hand, when the N content is more than 0.012 mass%, a hole called blister is generated in the steel sheet in the cold rolling. Accordingly, the N content is set to 0.002 mass% to 0.012 mass%. The N content is preferably 0.010% mass% or less in order to further reduce the blister.
- MnS precipitate is an important element forming a MnS precipitate through reacting with Mn.
- the MnS precipitate mainly affects the primary recrystallization and functions to suppress the variation depending on site in grain growth in the primary recrystallization due to the hot rolling.
- the Mn content is set to 0.001 mass% to 0.010 mass%.
- the Mn content is preferably 0.009 mass% or less in order to further improve the magnetic property.
- P increases the specific resistance of the grain-oriented electrical steel sheet to reduce the core loss.
- the P content is less than 0.01 mass%, the effect cannot be sufficiently obtained.
- the P content is more than 0.08 mass%, the cold rolling may become difficult to perform. Accordingly, the P content is set to 0.01 mass% to 0.08 mass%.
- Ti forms a TiN precipitate through reacting with N.
- Cu forms a CuS precipitate through reacting with S.
- These precipitates function to make the growth of the crystal grains in the finish annealing uniform irrespective of the site of the coil and suppress the variation in magnetic property of the grain-oriented electrical steel sheet.
- the TiN precipitate is considered to suppress the variation in grain growth in a high temperature region in the finish annealing to decrease the deviation of the magnetic property of the grain-oriented electrical steel sheet.
- the CuS precipitate is considered to suppress the variation in grain growth in a low temperature region in the decarburization annealing and the finish annealing to decrease the deviation of the magnetic property of the grain-oriented electrical steel sheet.
- the Ti content is less than 0.0020 mass% and the Cu content is less than 0.010 mass%, the effects cannot be sufficiently obtained.
- the Ti content is more than 0.010 mass%, the TiN precipitate is excessively formed and remains even after the finish annealing.
- the Cu content is more than 0.50 mass%, the CuS precipitate is excessively formed and remains even after the finish annealing. If these precipitates remain in the grain-oriented electrical steel sheet, it is difficult to obtain a high magnetic property.
- the molten steel contains one or both of Ti and Cu in ranges of Ti: 0.010 mass% or less and Cu: 0.50 mass% or less to satisfy at least one of Ti: 0.0020 mass% or more or Cu: 0.010 mass% or more.
- the molten steel contains at least one kind selected from a group consisting of Ti: 0.0020 mass% to 0.010 mass% and Cu: 0.010 mass% to 0.50 mass%.
- the lower limit of the Ti content is preferably 0.0020 mass%, and the upper limit of the Ti content is preferably 0.0080 mass%.
- the lower limit of the Cu content is preferably 0.01 mass%, and the upper limit of the Cu content is preferably 0.10 mass%.
- the Ti content (mass%) is expressed as [Ti] and the Cu content (mass%) is expressed as [Cu]
- it is more preferable that the relation of "20 ⁇ [Ti] + [Cu] ⁇ 0.18" is established and, preferably, the relation of "10 ⁇ [Ti] + [Cu] ⁇ 0.07" is established.
- each of the Cr content and the Sn content is preferably 0.20 mass% or less. Further, in order to sufficiently obtain the above effects, each of the Cr content and the Sn content is preferably 0.01 mass% or more. Note that Sn is a grain boundary segregation element and thus also has an effect to stabilize secondary recrystallization.
- the molten steel may contain Sb: 0.010 mass% to 0.20 mass%, Ni: 0.010 mass% to 0.20 mass%, Se: 0.005 mass% to 0.02 mass%, Bi: 0.005 mass% to 0.02 mass%, Pb: 0.005 mass% to 0.02 mass%, B: 0.005 mass% to 0.02 mass%, V: 0.005 mass% to 0.02 mass%, Mo: 0.005 mass% to 0.02 mass%, and/or As: 0.005 mass% to 0.02 mass%.
- These elements may be inhibitor strengthening elements.
- the slab is heated (Step S2).
- the temperature of the heating is preferably set to 1250°C or lower from the viewpoint of energy saving.
- the thickness of the hot-rolled steel sheet is not particularly limited, and may be set to 1.8 mm to 3.5 mm.
- annealing is performed on the hot-rolled steel sheet to obtain an annealed steel sheet (Step S4).
- the condition of the annealing is not particularly limited, and the annealing may be performed, for example, at a temperature of 750°C to 1200°C for 30 seconds to 10 minutes. The annealing improves the magnetic property.
- Step S5 cold rolling is performed on the annealed steel sheet to obtain a cold-rolled steel sheet.
- the cold rolling may be performed only once or a plurality of times while an intermediate annealing is performed therebetween.
- the intermediate annealing is preferably performed at a temperature of 750°C to 1200°C for 30 seconds to 10 minutes.
- the cold rolling is performed without performing the above-described intermediate annealing, it may be difficult to obtain uniform properties.
- the cold rolling is performed a plurality of times while the intermediate annealing is performed therebetween, the uniform properties are easily obtained but the magnetic flux density may decrease. Accordingly, it is preferable to determine the number of times of the cold rolling and the presence or absence of the intermediate annealing according to the property required for and the cost of the finally obtained grain-oriented electrical steel sheet.
- the rolling reduction at the final cold rolling it is preferable to set the rolling reduction at the final cold rolling to 80% to 95%.
- the decarburization annealing and nitridation annealing (decarburization and nitridation annealing) is performed on the cold-rolled steel sheet in a decarburizing and nitriding atmosphere after the cold rolling to obtain a decarburized nitrided steel sheet (Step S6).
- the decarburization annealing removes carbon in the steel sheet and causes primary recrystallization. Further, the nitridation annealing increases the nitrogen content in the steel sheet.
- An example of the decarburizing and nitriding atmosphere is a moist atmosphere containing hydrogen, nitrogen, water vapor and gas (ammonia or the like) having a nitriding capability.
- the present application discloses a decarburization and nitridation annealing, wherein at least the heating of the cold-rolled steel sheet is started in the decarburizing and nitriding atmosphere, then a first annealing is performed at a temperature T1 within a range of 700°C to 950°C, and then a second annealing is performed at a temperature T2. More specifically, the atmosphere containing the gas having the nitriding capability is prepared prior to the generation of decarburization, and the decarburization and the nitridation are simultaneously performed.
- the temperature T2 here is a temperature within a range of 850°C to 950°C when the temperature T1 is lower than 800°C, and is a temperature within a range of 800°C to 950°C when the temperature T1 is 800°C or higher. Further, it is preferable to keep the cold-rolled steel sheet at the temperature T1 and at the temperature T2 for 15 seconds or more each.
- the decarburization, primary recrystallization, and nitridation may occur in both of the annealing at the temperature T1 and the annealing at the temperature T2, and the annealing at the temperature T1 mainly contributes to nitridation and the annealing at the temperature T2 mainly contributes to appearance of the primary recrystallization.
- the crystal grain obtained through the primary recrystallization (primary recrystallized grain) is small so that the subsequent secondary recrystallization does not sufficiently appear.
- the temperature T1 is higher than 950°C, the primary recrystallized grain is large so that the subsequent secondary recrystallization does not sufficiently appear.
- the temperature T2 is lower than 850°C when the temperature T1 is lower than 800°C, the crystal grain (primary recrystallized grain) obtained through the primary recrystallization is small so that the subsequent secondary recrystallization does not sufficiently appear.
- the nitridation may be insufficient or the primary recrystallized grain may be small.
- the nitridation is likely to be insufficient
- the holding time at the temperature T2 is shorter than 15 seconds, the primary recrystallized grain with a sufficient size is less likely to be obtained.
- the temperature T2 may be made equal to the temperature T1. In other words, if the temperature T1 is 800°C or higher, the annealing at the temperature T1 and the annealing at the temperature T2 may be continuously performed. Further, when the temperature T1 and the temperature T2 are made different, it is preferable to set the temperature T1 to a temperature suitable for nitridation and set the temperature T2 to a temperature suitable for appearance of the primary recrystallization. Setting the temperature T1 and the second temperature T2 as described above makes it possible to further increase the magnetic flux density and further suppress the variation in magnetic flux density.
- the temperature T1 is set to a temperature in a range of 700°C to 850°C
- the temperature T2 is set to a temperature in a range of 850°C to 950°C.
- the first and the second decarburization and nitridation annealing are performed for 15 seconds or more, respectively.
- the temperature T1 falls within the range of 700°C to 850°C, it is possible to particularly effectively diffuse the nitrogen entering the surface of the steel sheet to the central portion of the steel sheet. Accordingly, the secondary recrystallization sufficiently appears and an excellent magnetic property is obtained. Further, when the temperature T2 falls within the range of 850°C to 950°C, it is possible to adjust the primary recrystallized grain to a particularly preferable size. Accordingly, the secondary recrystallization sufficiently appears and an excellent magnetic property is obtained.
- an annealing separating agent containing MgO as a main component is applied, in a water slurry, to the surface of the decarburized nitrided steel sheet, and the decarburized nitrided steel sheet is coiled. Then, batch-type finish annealing is performed on the coiled decarburized nitrided steel sheet to obtain a coiled finish-annealed steel sheet (Step S7).
- the finish annealing causes secondary recrystallization.
- Step S8 a coating solution containing aluminum phosphate and colloidal silica as main components is applied to the surface of the finish-annealed steel sheet, and baking is performed thereon to form an insulating film.
- the grain-oriented electrical steel sheet can be manufactured.
- the steel being an object for the hot rolling is not limited to the slab obtained through casting of the molten steel, but a so-called thin slab may be used. Further, when using the thin slab, it is not always necessary to perform the slab heating at 1250°C or lower.
- annealing was performed on the hot-rolled steel sheets at 1100°C for 120 seconds to obtain annealed steel sheets. Then, acid pickling was performed on the annealed steel sheets, and then cold rolling was performed on the annealed steel sheets to obtain cold-rolled steel sheets with a thickness of 0.23 mm. Subsequently, decarburization annealing and nitridation annealing (decarburization and nitridation annealing) was performed on the cold-rolled steel sheets in an atmosphere containing water vapor, hydrogen, nitrogen and ammonia to obtain decarburized nitrided steel sheets. In the decarburization and nitridation annealing, annealing was performed at a temperature T1 of 800°C to 840°C for 40 seconds, and then annealing was performed at 870°C for 70 seconds.
- an annealing separating agent containing MgO as a main component was applied, in a water slurry, to the surfaces of the decarburized nitrided steel sheets. Then, finish annealing was performed on them at 1200°C for 20 hours to obtain finish-annealed steel sheets. Subsequently, the finish-annealed steel sheets were washed with water, and then cutout into a single-plate magnetic measurement size with a width of 60 mm and a length of 300 mm. Subsequently, a coating solution containing aluminum phosphate and colloidal silica as main components was applied to the surfaces of the finish-annealed steel sheets, and baking was performed thereon to form an insulating film. In this manner, samples of the grain-oriented electrical steel sheets were obtained.
- the magnetic flux density B8 of each of the grain-oriented electrical steel sheets was measured.
- the magnetic flux density B8 is the magnetic flux density occurring in the grain-oriented electrical steel sheet when a magnetic field of 800 A/m at 50 Hz is applied thereto as described above.
- the magnetic flux densities B8 of five single-plate samples for measurement were measured for each of the samples.
- the average value "average B8,” the maximum value “B8max,” and the minimum value “B8min” were obtained.
- the difference “ ⁇ B8” between the maximum value "B8max” and the minimum value “B8min” was also obtained.
- the difference " ⁇ B8” is an index indicating the fluctuation range of the magnetic property.
- Fig. 1 the evaluation results based on the average value "average B8" and the difference " ⁇ B8” are indicated in Fig. 1 .
- an open circle mark in Fig. 1 indicates that the average value "average B8” was 1.90 T or more and the difference " ⁇ B8" was 0.030 T or less.
- a filled circle mark in Fig. 1 indicates that the average value "average B8" was less than 1.90 T or the difference " ⁇ B8" was more than 0.030 T.
- the average value "average B8" was large to be 1.90 T or more and the difference " ⁇ B8" was small to be 0.030 T or less. In short, high magnetic property was obtained and the variation in magnetic property was small.
- the balance between the average value "average B8" and the difference " ⁇ B8” was excellent in the samples No. 11, No. 13, and No. 15, in which the relation of "20 ⁇ [Ti]+[Cu] ⁇ 0.18" was established where the Ti content (mass%) was expressed as [Ti] and the Cu content (mass%) was expressed as [Cu].
- the balance between the average value "average B8" and the difference " ⁇ B8” was extremely excellent in the sample No. 15, in which the relation of "10 ⁇ [Ti]+[Cu] ⁇ 0.07" was established.
- annealing was performed on the hot-rolled steel sheets at 1090°C for 120 seconds to obtain annealed steel sheets. Then, acid pickling was performed on the annealed steel sheets, and then cold rolling was performed on the annealed steel sheets to obtain cold-rolled steel sheets with a thickness of 0.23 mm. Subsequently, steel sheets for annealing were cutout from the cold-rolled steel sheets, and decarburization annealing and nitridation annealing (decarburization and nitridation annealing) was performed on the steel sheets in an atmosphere containing water vapor, hydrogen, nitrogen and ammonia to obtain decarburized nitrided steel sheets. In the decarburization and nitridation annealing, annealing was performed at 800°C for 50 seconds, and then annealing was performed at temperatures T2 listed in Table 2 for 80 seconds.
- an annealing separating agent containing MgO as a main component was applied, in a water slurry, to the surfaces of the decarburized nitrided steel sheets. Then, finish annealing was performed on them at 1200°C for 20 hours to obtain finish-annealed steel sheets. Subsequently, treatments from the water washing to the formation of the insulating film were performed similarly to the first experiment to obtain samples of the grain-oriented electrical steel sheets.
- the average value "average B8" was large to be 1.90 T or more and the difference " ⁇ B8" was small to be 0.030 T or less. In short, a high magnetic property was obtained and the variation in the magnetic property was small.
- annealing was performed on the hot-rolled steel sheets at 1070°C for 120 seconds to obtain annealed steel sheets. Then, acid pickling was performed on the annealed steel sheets, and then cold rolling was performed on the annealed steel sheets to obtain cold-rolled steel sheets with a thickness of 0.23 mm. Subsequently, steel sheets for annealing were cutout from the cold-rolled steel sheets, and decarburization annealing and nitridation annealing (decarburization and nitridation annealing) was performed on the steel sheets in an atmosphere containing water vapor, hydrogen, nitrogen and ammonia to obtain decarburized nitrided steel sheets.
- decarburization annealing and nitridation annealing decarburization and nitridation annealing
- annealing was performed at temperatures T1 within a range of 680°C to 860°C listed in Table 3 for 20 seconds, and then annealing was performed at temperatures T2 within a range of 830°C to 960°C listed in Table 3 for 90 seconds.
- an annealing separating agent containing MgO as a main component was applied, in a water slurry, to the surfaces of the decarburized nitrided steel sheets. Then, finish annealing was performed on them at 1200°C for 20 hours to obtain finish-annealed steel sheets. Subsequently, treatments from the water washing to the formation of the insulating film were performed similarly to the first experiment to obtain samples of the grain-oriented electrical steel sheets.
- the average value "average B8" was large to be 1.90 T or more and the difference " ⁇ B8" was small to be 0.030 T or less. In short, a high magnetic property was obtained and the variation in the magnetic property was small.
- the average value "average B8" was particularly large to be 1.91T or more and the difference " ⁇ B8" was particularly small to be 0.025T or less.
- annealing was performed on the hot-rolled steel sheets at 1100°C for 120 seconds to obtain annealed steel sheets. Then, acid pickling was performed on the annealed steel sheets, and then cold rolling was performed on the annealed steel sheets to obtain cold-rolled steel sheets with a thickness of 0.23 mm. Subsequently, decarburization annealing and nitridation annealing (decarburization and nitridation annealing) was performed on the cold-rolled steel sheets in an atmosphere containing water vapor, hydrogen, nitrogen and ammonia to obtain decarburized nitrided steel sheets. In the decarburization and nitridation annealing, annealing was performed at temperatures T1 of 800°C to 840°C for 30 seconds, and then annealing was performed at 860°C for 80 seconds.
- an annealing separating agent containing MgO as a main component was applied, in a water slurry, to the surfaces of the decarburized nitrided steel sheets. Then, finish annealing was performed on them at 1200°C for 20 hours to obtain finish-annealed steel sheets. Subsequently, treatments from the water washing to the formation of the insulating film were performed similarly to the first experiment to obtain samples of the grain-oriented electrical steel sheets.
- the average value "average B8" was large to be 1.90 T or more and the difference " ⁇ B8" was small to be 0.30 T or less. In short, a high maghetic property was obtained and the variation in the magnetic property was small.
- the average value "average B8" was particularly large to be 1.91 T or more and the difference " ⁇ B8" was particularly small to be 0.025 T or less.
- the present invention is applicable, for example, in electrical steel sheet manufacturing industries and electrical steel sheet using industries.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Thermal Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electromagnetism (AREA)
- Manufacturing & Machinery (AREA)
- Dispersion Chemistry (AREA)
- Power Engineering (AREA)
- Manufacturing Of Steel Electrode Plates (AREA)
- Soft Magnetic Materials (AREA)
- Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
Claims (5)
- Procédé de fabrication d'une tôle d'acier électrique à grains orientés, comprenant :la mise en oeuvre d'un laminage à chaud sur un acier contenant Si : 2,5 % en masse à 4,0 % en masse, C : 0,02 % en masse à 0,10 % en masse, Mn : 0,05 % en masse à 0,20 % en masse, Al soluble dans les acides : 0,020 % en masse à 0,040 % en masse, N : 0,002 % en masse à 0,012 % en masse, S : 0,001 % en masse à 0,010 % en masse, et P : 0,01 % en masse à 0,08 % en masse, contenant en outre au moins un type choisi dans l'ensemble constitué par Ti : 0,0020 % en masse à 0,010 % en masse et Cu : 0,010 % en masse à 0,50 % en masse, lequel acier contient éventuellement au moins un type d'élément choisi dans l'ensemble constitué par Cr : 0,20 % en masse ou moins, Sn : 0,20 % en masse ou moins, Sb : 0,010 % en masse à 0,20 % en masse, Ni : 0,010 % en masse à 0,20 % en masse, Se : 0,005 % en masse à 0,02 % en masse, Bi : 0,005 % en masse à 0,02 % en masse, Pb : 0,005 % en masse à 0,02 % en masse, B : 0,005 % en masse à 0,02 % en masse, V : 0,005 % en masse à 0,02 % en masse, Mo : 0,005 % en masse à 0,02 % en masse, et/ou As : 0,005 % en masse à 0,02 % en masse, le reste étant composé de Fe et d'impuretés inévitables, pour que soit obtenue une tôle laminée à chaud ;
la mise en oeuvre d'un recuit sur la tôle d'acier laminée à chaud pour que soit obtenue une tôle d'acier recuite ;la mise en oeuvre d'un laminage à froid sur la tôle d'acier recuite pour que soit obtenue une tôle d'acier laminée à froid ;la mise en oeuvre d'un recuit par décarburation et nitruration sur la tôle d'acier laminée à froid pour que soit obtenue une tôle d'acier décarburée nitrurée ; etla mise en oeuvre d'un recuit de finition sur la tôle d'acier décarburée nitrurée,dans lequel l'étape pour obtenir la tôle d'acier décarburée nitrurée comprend :le démarrage d'un chauffage sur la tôle d'acier laminée à froid dans une atmosphère décarburante et nitrurante ;ensuite la mise en oeuvre d'un premier recuit par décarburation et nitruration à une première température pendant 15 secondes ou plus ; etensuite la mise en oeuvre d'un deuxième recuit par décarburation et nitruration à une deuxième température pendant 15 secondes ou plus,la première température étant située dans la plage allant de 700 °C à 850 °C, et
la deuxième température étant située dans la plage allant de 850 °C à 950° C. - Procédé de fabrication d'une tôle d'acier électrique à grains orientés, comprenant :la mise en oeuvre d'un laminage à chaud sur un acier contenant Si : 2,5 % en masse à 4,0 % en masse, C : 0,02 % en masse à 0,10 % en masse, Mn : 0,05 % en masse à 0,20 % en masse, Al soluble dans les acides : 0,020 % en masse à 0,040 % en masse, N : 0,002 % en masse à 0,012 % en masse, S : 0,001 % en masse à 0,010 % en masse, et P : 0,01 % en masse à 0,08 % en masse, contenant en outre l'un ou les deux parmi Ti et Cu à raison de Ti : 0,010 % en masse ou moins et Cu : 0,50 % en masse ou moins et de manière à satisfaire à au moins l'un parmi Ti : 0,0020 % en masse et Cu : 0,010 % en masse, lequel acier contient éventuellement au moins un type d'élément choisi dans l'ensemble constitué par Cr : 0,20 % en masse ou moins, Sn : 0,20 % en masse ou moins, Sb : 0,010 % en masse à 0,20 % en masse, Ni : 0,010 % en masse à 0,20 % en masse, Se : 0,005 % en masse à 0,02 % en masse, Bi : 0,005 % en masse à 0,02 % en masse, Pb : 0,005 % en masse à 0,02 % en masse, B : 0,005 % en masse à 0,02 % en masse, V : 0,005 % en masse à 0,02 % en masse, Mo : 0,005 % en masse à 0,02 % en masse, et/ou As : 0,005 % en masse à 0,02 % en masse, le reste étant composé de Fe et d'impuretés inévitables, pour que soit obtenue une tôle laminée à chaud ;la mise en oeuvre d'un recuit sur la tôle d'acier laminée à chaud pour que soit obtenue une tôle d'acier recuite ;la mise en oeuvre d'un laminage à froid sur la tôle d'acier recuite pour que soit obtenue une tôle d'acier laminée à froid ;la mise en oeuvre d'un recuit par décarburation et nitruration sur la tôle d'acier laminée à froid pour que soit obtenue une tôle d'acier décarburée nitrurée ; etla mise en oeuvre d'un recuit de finition sur la tôle d'acier décarburée nitrurée,dans lequel l'étape pour obtenir la tôle d'acier décarburée nitrurée comprend :le démarrage d'un chauffage sur la tôle d'acier laminée à froid dans une atmosphère décarburante et nitrurante ;ensuite la mise en oeuvre d'un premier recuit par décarburation et nitruration à une première température pendant 15 secondes ou plus ; etensuite la mise en oeuvre d'un deuxième recuit par décarburation et nitruration à une deuxième température pendant 15 secondes ou plus,la première température étant située dans la plage allant de 700 °C à 850 °C, etla deuxième température étant située dans la plage allant de 850°C à 950°C.
- Procédé de fabrication d'une tôle d'acier électrique à grains orientés selon la revendication 1 ou 2, dans lequel
la teneur en Ti de l'acier est de 0,0020 % en masse à 0,0080 % en masse,
la teneur en Cu de l'acier est de 0,01 % en masse à 0,10 % en masse, et
une relation "20 × [Ti] + [Cu] ≤ 0,18" est établie, où la teneur en Ti (% en masse) de l'acier est représentée par [Ti] et la teneur en Cu (% en masse) de l'acier est représentée par [Cu]. - Procédé de fabrication d'une tôle d'acier électrique à grains orientés selon la revendication 3, dans lequel une relation "10 × [Ti] + [Cu] ≤ 0,07" est établie.
- Procédé de fabrication d'une tôle d'acier électrique à grains orientés selon l'une quelconque des revendications 1 à 4, dans lequel le laminage à chaud sur l'acier est effectué après chauffage de l'acier à une température de 1 250 °C ou moins.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL11744741T PL2537946T3 (pl) | 2010-02-18 | 2011-02-18 | Sposób wytwarzania blachy cienkiej ze stali elektrotechnicznej o ziarnach zorientowanych |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010033906 | 2010-02-18 | ||
PCT/JP2011/053488 WO2011102455A1 (fr) | 2010-02-18 | 2011-02-18 | Procédé de fabrication d'une feuille en acier électromagnétique à grains orientés |
Publications (3)
Publication Number | Publication Date |
---|---|
EP2537946A1 EP2537946A1 (fr) | 2012-12-26 |
EP2537946A4 EP2537946A4 (fr) | 2014-05-07 |
EP2537946B1 true EP2537946B1 (fr) | 2019-08-07 |
Family
ID=44483040
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP11744741.7A Active EP2537946B1 (fr) | 2010-02-18 | 2011-02-18 | Procédé de fabrication d'une tôle d'acier électrique à grains orientés |
Country Status (8)
Country | Link |
---|---|
US (1) | US9175362B2 (fr) |
EP (1) | EP2537946B1 (fr) |
JP (1) | JP4943560B2 (fr) |
KR (1) | KR101322505B1 (fr) |
CN (1) | CN102762751B (fr) |
BR (1) | BR112012020687B1 (fr) |
PL (1) | PL2537946T3 (fr) |
WO (1) | WO2011102455A1 (fr) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011158519A1 (fr) * | 2010-06-18 | 2011-12-22 | Jfeスチール株式会社 | Procédé de production de plaques d'acier électromagnétiques orientées |
US10900113B2 (en) | 2014-09-04 | 2021-01-26 | Jfe Steel Corporation | Method for manufacturing grain-oriented electrical steel sheet, and nitriding apparatus |
KR101633255B1 (ko) | 2014-12-18 | 2016-07-08 | 주식회사 포스코 | 방향성 전기강판 및 그 제조방법 |
PL3358031T3 (pl) * | 2015-09-28 | 2020-12-28 | Nippon Steel Corporation | Blacha cienka ze stali elektrotechnicznej o ziarnach zorientowanych i blacha stalowa cienka walcowana na gorąco na blachę cienką ze stali elektrotechnicznej o ziarnach zorientowanych |
KR20170073311A (ko) * | 2015-12-18 | 2017-06-28 | 주식회사 포스코 | 방향성 전기강판용 절연피막 조성물, 방향성 전기강판의 절연피막 형성 방법, 및 절연피막이 형성된 방향성 전기강판 |
CN108699619B (zh) | 2016-02-22 | 2020-07-14 | 杰富意钢铁株式会社 | 方向性电磁钢板的制造方法 |
RU2697115C1 (ru) | 2016-03-09 | 2019-08-12 | ДжФЕ СТИЛ КОРПОРЕЙШН | Способ производства текстурированного стального листа из электротехнической стали |
CN113272454B (zh) * | 2019-01-16 | 2023-04-18 | 日本制铁株式会社 | 方向性电磁钢板的制造方法 |
EP4026921A4 (fr) * | 2019-09-06 | 2023-11-01 | JFE Steel Corporation | Tôle d'acier électromagnétique à grains orientés et procédé de production associé |
CN112410722B (zh) * | 2020-11-02 | 2022-11-29 | 哈尔滨工程大学 | 一种基于冷成型复合低温氮化处理的α+β型钛合金及其氮化层形成方法 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6451128B1 (en) * | 1997-06-27 | 2002-09-17 | Pohang Iron & Steel Co., Ltd. | Method for manufacturing high magnetic flux denshy grain oriented electrical steel sheet based on low temperature slab heating method |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0326912B1 (fr) | 1988-02-03 | 1994-07-27 | Nippon Steel Corporation | Procédé de fabrication d'une tôle en acier électrique à grain orienté présentant une haute densité de flux |
JPH0686632B2 (ja) * | 1988-02-03 | 1994-11-02 | 新日本製鐵株式会社 | 磁束密度の高い一方向性珪素鋼板の製造方法 |
JPH02200733A (ja) * | 1989-01-31 | 1990-08-09 | Nippon Steel Corp | 高磁束密度方向性電磁鋼板の製造方法 |
JP2603130B2 (ja) * | 1989-05-09 | 1997-04-23 | 新日本製鐵株式会社 | 高磁束密度方向性電磁鋼板の製造法 |
JPH03122227A (ja) | 1989-10-05 | 1991-05-24 | Nippon Steel Corp | 方向性電磁鋼板の脱炭連続焼鈍炉 |
JP3065853B2 (ja) * | 1992-12-08 | 2000-07-17 | 新日本製鐵株式会社 | 磁気特性の優れた一方向性電磁鋼板の安定製造方法 |
JPH07252531A (ja) | 1994-03-14 | 1995-10-03 | Nippon Steel Corp | 方向性珪素鋼板の製造方法 |
JP3056970B2 (ja) * | 1995-04-07 | 2000-06-26 | 新日本製鐵株式会社 | 磁気特性が優れた一方向性電磁鋼板の製造方法 |
IT1290977B1 (it) | 1997-03-14 | 1998-12-14 | Acciai Speciali Terni Spa | Procedimento per il controllo dell'inibizione nella produzione di lamierino magnetico a grano orientato |
JP4268277B2 (ja) * | 1999-07-29 | 2009-05-27 | 新日本製鐵株式会社 | 一方向性電磁鋼板の製造方法 |
CN100389222C (zh) * | 2005-12-13 | 2008-05-21 | 武汉钢铁(集团)公司 | 提高含铜取向硅钢电磁性能和底层质量的生产方法 |
JP4823719B2 (ja) * | 2006-03-07 | 2011-11-24 | 新日本製鐵株式会社 | 磁気特性が極めて優れた方向性電磁鋼板の製造方法 |
JP4598702B2 (ja) | 2006-03-23 | 2010-12-15 | 新日本製鐵株式会社 | 磁気特性が優れた高Si含有方向性電磁鋼板の製造方法 |
KR100817168B1 (ko) | 2006-12-27 | 2008-03-27 | 주식회사 포스코 | 자성이 우수한 방향성 전기강판의 제조방법 |
WO2008078915A1 (fr) * | 2006-12-27 | 2008-07-03 | Posco | Procédé de fabrication de tôles en acier magnétiques à grains orientés ayant une excellente propriété magnétique et une grande productivité |
WO2008078947A1 (fr) | 2006-12-27 | 2008-07-03 | Posco | Procédé de fabrication de tôles d'acier magnétiques à grains orientés |
JP5793305B2 (ja) | 2007-12-28 | 2015-10-14 | ポスコ | 磁気特性に優れた方向性電磁鋼板及びその製造方法 |
JP4608562B2 (ja) | 2008-03-05 | 2011-01-12 | 新日本製鐵株式会社 | 著しく磁束密度が高い方向性電磁鋼板の製造方法 |
JP5428188B2 (ja) * | 2008-04-15 | 2014-02-26 | 新日鐵住金株式会社 | 方向性電磁鋼板の製造方法 |
-
2011
- 2011-02-18 PL PL11744741T patent/PL2537946T3/pl unknown
- 2011-02-18 CN CN201180009917.2A patent/CN102762751B/zh active Active
- 2011-02-18 EP EP11744741.7A patent/EP2537946B1/fr active Active
- 2011-02-18 KR KR1020127024192A patent/KR101322505B1/ko active IP Right Grant
- 2011-02-18 US US13/579,692 patent/US9175362B2/en active Active
- 2011-02-18 WO PCT/JP2011/053488 patent/WO2011102455A1/fr active Application Filing
- 2011-02-18 BR BR112012020687-7A patent/BR112012020687B1/pt active IP Right Grant
- 2011-02-18 JP JP2011524095A patent/JP4943560B2/ja active Active
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6451128B1 (en) * | 1997-06-27 | 2002-09-17 | Pohang Iron & Steel Co., Ltd. | Method for manufacturing high magnetic flux denshy grain oriented electrical steel sheet based on low temperature slab heating method |
Also Published As
Publication number | Publication date |
---|---|
PL2537946T3 (pl) | 2019-12-31 |
KR20120120441A (ko) | 2012-11-01 |
BR112012020687A2 (pt) | 2018-10-23 |
US9175362B2 (en) | 2015-11-03 |
JPWO2011102455A1 (ja) | 2013-06-17 |
WO2011102455A1 (fr) | 2011-08-25 |
EP2537946A1 (fr) | 2012-12-26 |
KR101322505B1 (ko) | 2013-10-28 |
EP2537946A4 (fr) | 2014-05-07 |
JP4943560B2 (ja) | 2012-05-30 |
CN102762751A (zh) | 2012-10-31 |
BR112012020687B1 (pt) | 2019-11-26 |
CN102762751B (zh) | 2016-04-13 |
US20120312424A1 (en) | 2012-12-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2537946B1 (fr) | Procédé de fabrication d'une tôle d'acier électrique à grains orientés | |
EP2537947B1 (fr) | Procédé de fabrication d'une tôle en acier électrique à grains orientés | |
EP2876173B9 (fr) | Procédé permettant de produire une tôle d'acier électrique à grains orientés | |
EP2548977B1 (fr) | Procédé de production d'une tôle d'acier électromagnétique directionnel | |
EP2578706B1 (fr) | Procédé de production d'une tôle d'acier magnétique a grains orientes | |
JP5757693B2 (ja) | 低鉄損一方向性電磁鋼板の製造方法 | |
EP2418294B1 (fr) | Procédé de traitement d'acier pour une tôle d'acier électrique à grains orientés et procédé de production d'une tôle d'acier électrique à grains orientés | |
EP4174194A1 (fr) | Procédé de production d'une tôle d'acier électrique à grains orientés | |
JP4608562B2 (ja) | 著しく磁束密度が高い方向性電磁鋼板の製造方法 | |
JP7365414B2 (ja) | 方向性電磁鋼板およびその製造方法 | |
JP7053848B2 (ja) | 方向性電磁鋼板およびその製造方法 | |
KR102319831B1 (ko) | 방향성 전기강판의 제조방법 | |
KR101568835B1 (ko) | 방향성 전기강판 및 그 제조방법 | |
JP2022006215A (ja) | 方向性電磁鋼板および方向性電磁鋼板の製造方法 | |
JP2019137881A (ja) | 方向性電磁鋼板の製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20120918 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: NIPPON STEEL & SUMITOMO METAL CORPORATION |
|
DAX | Request for extension of the european patent (deleted) | ||
A4 | Supplementary search report drawn up and despatched |
Effective date: 20140407 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C23C 8/80 20060101ALI20140401BHEP Ipc: H01F 1/16 20060101ALI20140401BHEP Ipc: C21D 8/12 20060101AFI20140401BHEP Ipc: C22C 38/16 20060101ALI20140401BHEP Ipc: C22C 38/34 20060101ALI20140401BHEP Ipc: C21D 3/04 20060101ALI20140401BHEP Ipc: C22C 38/06 20060101ALI20140401BHEP Ipc: C23C 8/02 20060101ALI20140401BHEP Ipc: C22C 38/04 20060101ALI20140401BHEP Ipc: C21D 9/46 20060101ALI20140401BHEP Ipc: C22C 38/00 20060101ALI20140401BHEP Ipc: C22C 38/02 20060101ALI20140401BHEP |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
17Q | First examination report despatched |
Effective date: 20170825 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R079 Ref document number: 602011061046 Country of ref document: DE Free format text: PREVIOUS MAIN CLASS: C21D0008120000 Ipc: C22C0033040000 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C21D 3/04 20060101ALI20190108BHEP Ipc: C22C 38/04 20060101ALI20190108BHEP Ipc: C22C 38/14 20060101ALI20190108BHEP Ipc: C22C 38/00 20060101ALI20190108BHEP Ipc: C23C 8/80 20060101ALI20190108BHEP Ipc: H01F 1/16 20060101ALI20190108BHEP Ipc: C22C 38/02 20060101ALI20190108BHEP Ipc: C22C 38/16 20060101ALI20190108BHEP Ipc: C21D 8/12 20060101ALI20190108BHEP Ipc: C23C 8/02 20060101ALI20190108BHEP Ipc: C22C 38/06 20060101ALI20190108BHEP Ipc: C21D 9/46 20060101ALI20190108BHEP Ipc: C22C 33/04 20060101AFI20190108BHEP Ipc: C22C 38/34 20060101ALI20190108BHEP |
|
INTG | Intention to grant announced |
Effective date: 20190211 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: NIPPON STEEL CORPORATION |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE PATENT HAS BEEN GRANTED |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP Ref country code: AT Ref legal event code: REF Ref document number: 1163976 Country of ref document: AT Kind code of ref document: T Effective date: 20190815 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 602011061046 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: MP Effective date: 20190807 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: HR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191107 Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191209 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: NO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191107 |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK05 Ref document number: 1163976 Country of ref document: AT Kind code of ref document: T Effective date: 20190807 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191207 Ref country code: RS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: ES Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: AL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191108 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: EE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: IT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: RO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SM Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200224 Ref country code: SK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: CZ Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 602011061046 Country of ref document: DE |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
PG2D | Information on lapse in contracting state deleted |
Ref country code: IS |
|
26N | No opposition filed |
Effective date: 20200603 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
REG | Reference to a national code |
Ref country code: BE Ref legal event code: MM Effective date: 20200229 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200218 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200229 Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200229 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200218 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200229 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190807 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: PL Payment date: 20231228 Year of fee payment: 14 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20231228 Year of fee payment: 14 Ref country code: GB Payment date: 20240109 Year of fee payment: 14 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20240103 Year of fee payment: 14 |